Basic Information | Post buying leads | Suppliers |
Name |
3'-Chloro-2-(diethylamino)-o-aceto toluidide hydrochloride |
EINECS | N/A |
CAS No. | 77966-46-2 | Density | N/A |
PSA | N/A | LogP | N/A |
Solubility | N/A | Melting Point |
N/A |
Formula | C13H20Cl2N2O | Boiling Point | 375.8 °C at 760 mmHg |
Molecular Weight | 291.221 | Flash Point | 181.1 °C |
Transport Information | N/A | Appearance | N/A |
Safety | Risk Codes | N/A | |
Molecular Structure | Hazard Symbols | N/A | |
Synonyms |
Acetanilide, 3-chloro-2-(diethylamino)-2-methyl-, hydrochloride;(3-chloro-2-methyl-phenyl)carbamoylmethyl-diethyl-azanium chloride;3-Chloro-2-(diethylamino)-o-acetotoluidide hydrochloride;C 3037;o-ACETOTOLUIDIDE, 3-CHLORO-2-(DIETHYLAMINO)-, HYDROCHLORIDE;2′-CHLORO-2-(DIETHYLAMINO)-2′-METHYL ACETANILIDE HYDROCHLORIDE; |
The 3'-Chloro-2-(diethylamino)-o-aceto toluidide hydrochloride, with CAS registry number 77966-46-2, has the systematic name of 2-[(3-chloro-2-methylphenyl)amino]-N,N-diethyl-2-oxoethanaminium chloride. And its classification codes are Drug / Therapeutic Agent, Skin / Eye Irritant.
Physical properties of 3'-Chloro-2-(diethylamino)-o-aceto toluidide hydrochloride: (1)ACD/LogP: 2.62; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): 0.18; (4)ACD/LogD (pH 7.4): 1.89; (5)ACD/BCF (pH 5.5): 1; (6)ACD/BCF (pH 7.4): 10.61; (7)ACD/KOC (pH 5.5): 2.29; (8)ACD/KOC (pH 7.4): 116.51; (9)#H bond acceptors: 3; (10)#H bond donors: 1; (11)#Freely Rotating Bonds: 5; (12)Polar Surface Area: 20.31 Å2; (13)Enthalpy of Vaporization: 62.33 kJ/mol; (14)Vapour Pressure: 7.6E-06 mmHg at 25°C.
You can still convert the following datas into molecular structure:
(1)SMILES: [Cl-].Clc1cccc(NC(=O)C[NH+](CC)CC)c1C
(2)InChI: InChI=1/C13H19ClN2O.ClH/c1-4-16(5-2)9-13(17)15-12-8-6-7-11(14)10(12)3;/h6-8H,4-5,9H2,1-3H3,(H,15,17);1H
(3)InChIKey: QUHMNMSROUSUOR-UHFFFAOYAF
(4)Std. InChI: InChI=1S/C13H19ClN2O.ClH/c1-4-16(5-2)9-13(17)15-12-8-6-7-11(14)10(12)3;/h6-8H,4-5,9H2,1-3H3,(H,15,17);1H
(5)Std. InChIKey: QUHMNMSROUSUOR-UHFFFAOYSA-N
The toxicity data is as follows:
Organism | Test Type | Route | Reported Dose (Normalized Dose) | Effect | Source |
---|---|---|---|---|---|
mouse | LD50 | intraperitoneal | 200mg/kg (200mg/kg) | Journal of the American Pharmaceutical Association, Scientific Edition. Vol. 49, Pg. 80, 1960. | |
mouse | LD50 | subcutaneous | 375mg/kg (375mg/kg) | Journal of the American Pharmaceutical Association, Scientific Edition. Vol. 49, Pg. 80, 1960. | |
rat | LD50 | intraperitoneal | 245mg/kg (245mg/kg) | Arzneimittel-Forschung. Drug Research. Vol. 8, Pg. 270, 1958. |